US5637115A - Oxidation hair dye compositions containing developers, couplers, and AZO dyes - Google Patents
Oxidation hair dye compositions containing developers, couplers, and AZO dyes Download PDFInfo
- Publication number
- US5637115A US5637115A US08/586,300 US58630096A US5637115A US 5637115 A US5637115 A US 5637115A US 58630096 A US58630096 A US 58630096A US 5637115 A US5637115 A US 5637115A
- Authority
- US
- United States
- Prior art keywords
- group
- amino
- formula
- hair dye
- percent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 239000000118 hair dye Substances 0.000 title claims abstract description 61
- 230000003647 oxidation Effects 0.000 title claims abstract description 34
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 34
- 239000000987 azo dye Substances 0.000 title claims abstract description 15
- 210000004209 hair Anatomy 0.000 claims abstract description 42
- 150000001875 compounds Chemical class 0.000 claims abstract description 38
- 239000000126 substance Substances 0.000 claims abstract description 29
- -1 p-aminophenyl group Chemical group 0.000 claims abstract description 20
- 239000000975 dye Substances 0.000 claims abstract description 15
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims abstract description 7
- 239000002562 thickening agent Substances 0.000 claims abstract description 7
- 125000003118 aryl group Chemical group 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims abstract description 5
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims abstract description 4
- ALQKEYVDQYGZDN-UHFFFAOYSA-N 2-amino-6-methylphenol Chemical compound CC1=CC=CC(N)=C1O ALQKEYVDQYGZDN-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims abstract description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
- 239000000460 chlorine Substances 0.000 claims abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 4
- 239000011737 fluorine Substances 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 4
- 239000001005 nitro dye Substances 0.000 claims abstract description 4
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000004094 surface-active agent Substances 0.000 claims abstract 6
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000000490 cosmetic additive Substances 0.000 claims abstract 3
- 239000011630 iodine Substances 0.000 claims abstract 3
- 229910052740 iodine Inorganic materials 0.000 claims abstract 3
- 238000004043 dyeing Methods 0.000 claims description 17
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 14
- 239000007800 oxidant agent Substances 0.000 claims description 13
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 8
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 7
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- 235000006708 antioxidants Nutrition 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 5
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 claims description 5
- 235000010323 ascorbic acid Nutrition 0.000 claims description 5
- 239000011668 ascorbic acid Substances 0.000 claims description 5
- 229960005070 ascorbic acid Drugs 0.000 claims description 5
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 5
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims description 4
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 4
- 239000006071 cream Substances 0.000 claims description 4
- 150000004665 fatty acids Chemical class 0.000 claims description 4
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 4
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 3
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 3
- OQWWMUWGSBRNMA-UHFFFAOYSA-N 1-(2,4-diaminophenoxy)ethanol Chemical compound CC(O)OC1=CC=C(N)C=C1N OQWWMUWGSBRNMA-UHFFFAOYSA-N 0.000 claims description 3
- 229940113489 2,4-diaminophenoxyethanol Drugs 0.000 claims description 3
- 229940075142 2,5-diaminotoluene Drugs 0.000 claims description 3
- BXBOXUNPNIJELB-UHFFFAOYSA-N 2,6-dimethoxypyridine-3,5-diamine Chemical compound COC1=NC(OC)=C(N)C=C1N BXBOXUNPNIJELB-UHFFFAOYSA-N 0.000 claims description 3
- KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 claims description 3
- SBUMIGFDXJIPLE-UHFFFAOYSA-N 2-(3-amino-4-methoxyanilino)ethanol Chemical compound COC1=CC=C(NCCO)C=C1N SBUMIGFDXJIPLE-UHFFFAOYSA-N 0.000 claims description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 3
- NZKTVPCPQIEVQT-UHFFFAOYSA-N 2-[4-[(4-aminophenyl)diazenyl]-n-(2-hydroxyethyl)anilino]ethanol Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C(N(CCO)CCO)C=C1 NZKTVPCPQIEVQT-UHFFFAOYSA-N 0.000 claims description 3
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 3
- 229940018563 3-aminophenol Drugs 0.000 claims description 3
- GRLQBYQELUWBIO-UHFFFAOYSA-N 4,6-dichlorobenzene-1,3-diol Chemical compound OC1=CC(O)=C(Cl)C=C1Cl GRLQBYQELUWBIO-UHFFFAOYSA-N 0.000 claims description 3
- PZKNKZNLQYKXFV-UHFFFAOYSA-N 4-amino-2-(aminomethyl)phenol Chemical compound NCC1=CC(N)=CC=C1O PZKNKZNLQYKXFV-UHFFFAOYSA-N 0.000 claims description 3
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 3
- GPMWAWDEZPFUTN-UHFFFAOYSA-N 4-fluoro-6-methylbenzene-1,3-diamine Chemical compound CC1=CC(F)=C(N)C=C1N GPMWAWDEZPFUTN-UHFFFAOYSA-N 0.000 claims description 3
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 claims description 3
- NLMQHXUGJIAKTH-UHFFFAOYSA-N 4-hydroxyindole Chemical compound OC1=CC=CC2=C1C=CN2 NLMQHXUGJIAKTH-UHFFFAOYSA-N 0.000 claims description 3
- SPNBXQUPIHKTMI-UHFFFAOYSA-N 5-amino-2-(1-hydroxyethoxy)phenol Chemical compound CC(O)OC1=CC=C(N)C=C1O SPNBXQUPIHKTMI-UHFFFAOYSA-N 0.000 claims description 3
- PERWLJUQQIWGLB-UHFFFAOYSA-N 5-amino-4-ethoxy-2-methylphenol Chemical compound CCOC1=CC(C)=C(O)C=C1N PERWLJUQQIWGLB-UHFFFAOYSA-N 0.000 claims description 3
- HEAQOCBITATQEW-UHFFFAOYSA-N 5-amino-4-fluoro-2-methylphenol Chemical compound CC1=CC(F)=C(N)C=C1O HEAQOCBITATQEW-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
- LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Chemical compound OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 239000003995 emulsifying agent Substances 0.000 claims description 3
- 229940018564 m-phenylenediamine Drugs 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 235000010265 sodium sulphite Nutrition 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- 239000000080 wetting agent Substances 0.000 claims description 3
- BYYOWEYWJDNTBJ-UHFFFAOYSA-N 2-[(4-methylphenyl)methyl]pyrazole-3,4-diamine Chemical compound C1=CC(C)=CC=C1CN1C(N)=C(N)C=N1 BYYOWEYWJDNTBJ-UHFFFAOYSA-N 0.000 claims description 2
- YFEMHKMJMXYQSB-UHFFFAOYSA-N 2-[4-[(4-aminophenyl)diazenyl]-3-chloro-n-(2-hydroxyethyl)anilino]ethanol Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C(N(CCO)CCO)C=C1Cl YFEMHKMJMXYQSB-UHFFFAOYSA-N 0.000 claims description 2
- YSVKKVUAUKQDBY-UHFFFAOYSA-N 2-[4-[(4-aminophenyl)diazenyl]-n-(2-hydroxyethyl)-3-methylanilino]ethanol Chemical compound CC1=CC(N(CCO)CCO)=CC=C1N=NC1=CC=C(N)C=C1 YSVKKVUAUKQDBY-UHFFFAOYSA-N 0.000 claims description 2
- URPJUMVYJFHGOR-UHFFFAOYSA-N 2-benzylpyrazole-3,4-diamine Chemical compound NC1=C(N)C=NN1CC1=CC=CC=C1 URPJUMVYJFHGOR-UHFFFAOYSA-N 0.000 claims description 2
- XOAXOKSJNVLLHZ-UHFFFAOYSA-N 2-methylpyrazole-3,4-diamine Chemical compound CN1N=CC(N)=C1N XOAXOKSJNVLLHZ-UHFFFAOYSA-N 0.000 claims description 2
- DAWNEUSXWHZHRZ-UHFFFAOYSA-N 2-propan-2-ylpyrazole-3,4-diamine Chemical compound CC(C)N1N=CC(N)=C1N DAWNEUSXWHZHRZ-UHFFFAOYSA-N 0.000 claims description 2
- FLROJJGKUKLCAE-UHFFFAOYSA-N 3-amino-2-methylphenol Chemical compound CC1=C(N)C=CC=C1O FLROJJGKUKLCAE-UHFFFAOYSA-N 0.000 claims description 2
- GHCDZDOSAZHYFL-UHFFFAOYSA-N 4-amino-2-(ethoxymethyl)phenol Chemical compound CCOCC1=CC(N)=CC=C1O GHCDZDOSAZHYFL-UHFFFAOYSA-N 0.000 claims description 2
- RGKJLNMYCNSVKZ-UHFFFAOYSA-N 4-amino-2-(methoxymethyl)phenol Chemical compound COCC1=CC(N)=CC=C1O RGKJLNMYCNSVKZ-UHFFFAOYSA-N 0.000 claims description 2
- AYAKPRUPZTWPLK-UHFFFAOYSA-N 4-ethoxy-6-methylbenzene-1,3-diamine Chemical compound CCOC1=CC(C)=C(N)C=C1N AYAKPRUPZTWPLK-UHFFFAOYSA-N 0.000 claims description 2
- WDQMXRWYXILWPT-UHFFFAOYSA-N 5-amino-4-chloro-2-methylphenol Chemical compound CC1=CC(Cl)=C(N)C=C1O WDQMXRWYXILWPT-UHFFFAOYSA-N 0.000 claims description 2
- 239000004166 Lanolin Substances 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- 239000005662 Paraffin oil Substances 0.000 claims description 2
- 239000004264 Petrolatum Substances 0.000 claims description 2
- 229920002472 Starch Chemical class 0.000 claims description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 229960003237 betaine Drugs 0.000 claims description 2
- 229910021538 borax Inorganic materials 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 239000001913 cellulose Chemical class 0.000 claims description 2
- 229920002678 cellulose Chemical class 0.000 claims description 2
- 235000012000 cholesterol Nutrition 0.000 claims description 2
- 229940039717 lanolin Drugs 0.000 claims description 2
- 235000019388 lanolin Nutrition 0.000 claims description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 2
- 229920000847 nonoxynol Polymers 0.000 claims description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 2
- 235000019161 pantothenic acid Nutrition 0.000 claims description 2
- 150000002948 pantothenic acids Chemical class 0.000 claims description 2
- 229940066842 petrolatum Drugs 0.000 claims description 2
- 235000019271 petrolatum Nutrition 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 claims description 2
- 101150108015 STR6 gene Proteins 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 230000037308 hair color Effects 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000982 direct dye Substances 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- KZTWOUOZKZQDMN-UHFFFAOYSA-N 2,5-diaminotoluene sulfate Chemical compound OS(O)(=O)=O.CC1=CC(N)=CC=C1N KZTWOUOZKZQDMN-UHFFFAOYSA-N 0.000 description 2
- 229940075147 2,5-diaminotoluene sulfate Drugs 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000003806 hair structure Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 description 1
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
- LHGQFZQWSOXLEW-UHFFFAOYSA-N 1h-pyrazole-4,5-diamine Chemical class NC=1C=NNC=1N LHGQFZQWSOXLEW-UHFFFAOYSA-N 0.000 description 1
- BQHMISUMCDYQTR-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-ylamino)ethanol Chemical compound OCCNC1=CC=C2OCOC2=C1 BQHMISUMCDYQTR-UHFFFAOYSA-N 0.000 description 1
- OJYWOOVHUFSZJP-UHFFFAOYSA-N 2-(4-nitroanilino)ethylurea Chemical class NC(=O)NCCNC1=CC=C([N+]([O-])=O)C=C1 OJYWOOVHUFSZJP-UHFFFAOYSA-N 0.000 description 1
- JHWKYZJXIHYBTL-UHFFFAOYSA-N 2-amino-4-chloro-6-methylphenol Chemical compound CC1=CC(Cl)=CC(N)=C1O JHWKYZJXIHYBTL-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 1
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
- TWLMSPNQBKSXOP-UHFFFAOYSA-N 6358-09-4 Chemical compound NC1=CC([N+]([O-])=O)=CC(Cl)=C1O TWLMSPNQBKSXOP-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- JSFUMBWFPQSADC-UHFFFAOYSA-N Disperse Blue 1 Chemical compound O=C1C2=C(N)C=CC(N)=C2C(=O)C2=C1C(N)=CC=C2N JSFUMBWFPQSADC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000000986 disperse dye Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 210000004919 hair shaft Anatomy 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- IPSIPYMEZZPCPY-UHFFFAOYSA-N new fuchsin Chemical compound [Cl-].C1=CC(=[NH2+])C(C)=CC1=C(C=1C=C(C)C(N)=CC=1)C1=CC=C(N)C(C)=C1 IPSIPYMEZZPCPY-UHFFFAOYSA-N 0.000 description 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000005691 oxidative coupling reaction Methods 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 229940031826 phenolate Drugs 0.000 description 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
Definitions
- the present invention relates to a composition for oxidative dyeing of hair based on a combination of developer and coupler substances and based on a yellow to yellow-orange azo dye compound.
- Oxidation hair dyes have attained substantial importance in hair dye practice.
- the hair dye is produced by oxidative coupling of developer substance and coupler substance on the hair shaft. This leads to a very intensive hair dyeing with very good color fastness.
- m-phenylenediamine and its derivatives such as 2,4-diaminophenoxyethanol, 2,4-diamino-5-fluorotoluene and 2-amino-4-(2'-hydroxyethyl)aminoanisole, or pyridine derivatives such as 3,5-diamino-2,6-dimethoxypyridine as blue couplers; 1-naphthol, m-aminophenol and its derivatives, such as 2-amino-4-chloro-6-methylphenol, 5-amino-2-methylphenol, 4-amino-2-hydroxyphenoxyethanol, 4-amino-5-fluoro-2-hydroxytoluene and 4-amino-5-ethoxy-2-hydroxytoluene as red couplers; and resorcinol, 4-chlororesorcinol, 4,6-dichlororesorcinol, 2-methylresorcinol, 4-hydroxy-1,2-methylenedioxybenzene, 4-(2'-hydroxyethyl
- an oxidation hair dye composition for oxidative dyeing of hair contains a combination of at least one coupler substance and at least one developer substance and includes at least one azo dye compound of the formula I,
- A is a p-aminophenyl group of the formula (II) or a 3-pyridyl group of the formula (III): ##STR2## wherein B is a 4-[N,N-bis-(2'-hydroxyethyl)amino]phenyl group of the formula IV: ##STR3## wherein R is hydrogen, an alkyl group with from 1 to 6 carbon atoms, fluorine, chlorine, bromine or iodine, or B is a 2,6-diamino-3-pyridyl group of the formula V: ##STR4##
- the at least one azo dye compound of the formula I has an A group according to the formula II or the formula III, if the B group is according to the formula V, but has an A group according to the formula II, if the B group is the B Group according to the formula IV.
- azo dye compounds 4-amino-4'-[N,N-bis-(2"-hydroxyethyl)amino]azobenzene, 4-amino-2'-methyl-4'-[N,N-bis-(2"-hydroxyethyl)amino]azobenzene, 4-amino-2'-chloro-4'-[N,N-bis-(2"-hydroxyethyl)amino]azobenzene and 2,6-diamino-3-[3'-azopyridyl]-pyridine.
- the azo dye compounds of formula I can be used in the hair dye composition according to the invention individually and also in a mixture with each other.
- the total amount of these compounds advantageously amounts to from about 0.01 to 2 percent by weight.
- An amount of from about 0.05 to 0.5 percent by weight of the azo dye compound of formula I is particularly preferred.
- the developer substance for the hair dye composition according to the invention can include one or more of the following: 1,4-diaminobenzene, 2,5-diaminotoluene, 2-(2'-hydroxyethyl)-1,4-diaminobenzene, 4-aminophenol, 4-amino-2-aminomethylphenol, 4-amino-3-methylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-ethoxymethylphenol, 4,5-diamino-1-methylpyrazole, 4,5-diamino-1-isopropyl pyrazole, 1-benzyl-4,5-diamino pyrazole, 4,5-diamino-1-(4'-methylbenzyl)pyrazole and tetraaminopyrimidine.
- developer substances can be used alone, or in a mixture with each other, and are contained in the hair dye composition according to the invention advantageously in an amount of from 0.01 to 10 percent by weight, particularly advantageously however from 0.05 to 5.0 percent by weight.
- the coupler substance in the hair dye composition according to the invention can include one or more of the following coupler compounds: resorcinol, 4-chlororesorcinol, 4,6-dichlororesorcinol, 2-methylresorcinol, 2-amino-4-(2'-hydroxyethylamino)anisole, 2,4-diamino-5-fluorotoluene, m-phenylenediamine, 5-amino-2-methylphenol, 2,4-diaminophenoxyethanol, 1-naphthol, m-aminophenol, 3-amino-4-chloro-6-methylphenol, 3-amino-2-methylphenol, 4-amino-2-hydroxyphenoxyethanol, 4-amino-5-fluoro-2-hydroxytoluene, 4-amino-5-ethoxy-2-hydroxytoluene, 4-hydroxy-1,2-methylenedioxybenzene, 4-(2'-hydroxyethylamino)-1,2-methylenedioxybenzene, 2,
- the coupler substance can be contained in the oxidation hair dye composition according to the invention in an amount from 0.01 to 5 percent by weight, advantageously 0.05 to 3 percent by weight.
- the total amount of the developer-coupler combination contained in the hair dye composition described here should amount to from about 0.1 to 6 percent by weight, but from about 0.5 to 4.0 percent by weight is particularly preferred.
- the developer substances are used generally in about equimolar quantities, relative to the coupler substances. It is however not disadvantageous when the developer substances are present in a certain excess relative to the coupler substances present or when the coupler substance is present in excess relative to the developer substances.
- direct dyes can also be included in the hair dye compositions according to the invention.
- These direct dyes can include, for example, 6-amino-2-methylphenol and 2-amino-5-methylphenol as well as additional conventional direct dyes, for example triphenylmethane dye compounds, such as 4-[(4'-aminophenyl)-(4"-imino-2",5"-cyclohexadien-1"-yliden)methyl]-2-methylaminobenzene monohydrochloride, otherwise known as Basic Violet 14 (C.I.
- aromatic nitro dye compounds such as 2-amino-4,6-dinitrophenol, 2-amino-5-(2'-hydroxyethylamino)-nitrobenzene and 4-(2'-hydroxyethylamino)-3-nitrotoluene, 1-(2'-ureidoethyl)amino-4-nitrobenzene and azo dye compounds, such as 7-[(4'-aminophenyl)azo]-8-hydroxynaphthalen-4-sulfonic acid sodium salt, otherwise known as Acid Brown 4 (C.I.
- disperse dye compounds such as 1,4-diaminoanthraquinone and 1,4,5,8-tetraaminoanthraquinone.
- These direct dye compounds can be included in the hair dye composition according to the invention in amounts of from 0.1 to 4.0 percent by weight.
- the coupler and developer substances and the other dye components in so far as they are bases, can be used understandably also in the form of physiologically acceptable or compatible acid addition salts, for example as their hydrochlorides or sulfates, or--in so far as they have aromatic OH groups--in the form of salts with bases, for example as an alkali metal phenolate.
- the hair dye compositions according to the invention can include antioxidants, such as ascorbic acid, sodium bisulfite, sodium sulfite or thioglycolic acid. These antioxidants are advantageously present in an amount of from about 0.1 to 1.5 percent by weight. The use of ascorbic acid, sodium sulfite and especially sodium bisulfite is particularly preferred.
- the preparation used can be for example in the form of a solution, especially an aqueous-alcoholic solution.
- the particularly preferred forms of the preparation are however a cream, a gel or an emulsion.
- composition of the preparation comprises a mixture of the above-described dye components with the conventional additives used in this type of cosmetic preparation.
- Additional standard additives for hair dye compositions according to the invention in the form of solutions, creams, emulsions or gels include, for example, solvents such as water, lower aliphatic alcohols such as ethanol, propanol, isopropanol and glycerol, or glycols, such as 1,2-propylene glycol; wetting agents or emulsifiers chosen from the categories of anionic, cationic, amphoteric or nonionic surface active substances, such as fatty alcohol sulfates, ethoxylated fatty alcohol sulfates, alkylsulfonates, alkylbenzene sulfonates, alkyltrimethylammonium salts, alkylbetains, ethoxylated fatty alcohols, ethoxylated nonylphenol, fatty acid alkanol amides, ethoxylated fatty acid esters; thickeners, such as higher fatty alcohols, starches, cellulose derivatives, Petrolat
- the above-mentioned conventional components are used in amounts which are standard for their particular purpose, e.g. the wetting agents and emulsifiers in concentrations of about 0.5 to 30 percent by weight, the thickeners in amounts of from about 0.1 to 25 percent by weight and the hair care materials in a concentration of about 0.1 to 5.0 percent by weight.
- the hair dye composition according to the invention can be weakly acidic, neutral or alkaline according to its composition.
- the pH of the hair dye composition particularly can be from 6.0 to 11.5.
- the pH of the composition can be adjusted successfully with ammonia, but it can also be adjusted with an organic amine, for example monoethanolamine and triethanolamine, or also an inorganic base, such as sodium hydroxide and potassium hydroxide.
- an organic amine for example monoethanolamine and triethanolamine
- an inorganic base such as sodium hydroxide and potassium hydroxide.
- phosphoric acid, acetic acid, citric acid or tartaric acid can be used.
- the method of using the oxidation hair dye composition according to the invention includes mixing the above-described hair dye composition immediately prior to use with an oxidizing agent and applying the mixture to the hair in a sufficient amount to dye the hair, according to the amount of hair present, generally in an amount of from 60 to 200 g.
- the oxidizing agent or composition for developing the hair dye includes principally hydrogen peroxide or its addition compounds with urea, melamine or sodium borate in the form of a 3 to 12 percent, advantageously 6 percent, aqueous solution.
- air oxygen can also be used.
- the weight ratio of hair dye composition according to the invention and oxidizing agent amounts to 5:1 to 1:2, advantageously however 1:1. Comparatively larger amounts of oxidizing agent are used particularly when there is a high dye compound concentration in the oxidation hair dye composition or when at the same time a comparatively stronger bleaching of the hair is intended.
- the mixture of the oxidizing agent and the hair dye composition is allowed to act on the hair at 15° to 50° C. for from 10 to 45 minutes, advantageously 30 minutes, the hair is rinsed with water and dried. If necessary in connection with the rinsing a shampoo is used to wash the hair and eventually an after-rinse is performed with a weak organic acid, such as citric acid or tartaric acid. Subsequently the hair is dried.
- a weak organic acid such as citric acid or tartaric acid.
- the hair dye compositions according to the invention provide hair colors of outstanding fastness properties, particular an outstanding light fastness, wash fastness and friction fastness and they may be removed with reducing agents. They also provide a broad palette of different hair color shades and nuances according to their type and composition, especially fashionable gold shades. Finally dyeing of gray and chemically undamaged hair is problem-free when the hair dye compositions according to the invention are used and a very good color coverage is obtained.
- the colors produced using the hair dye compositions according to the invention are both uniform and very satisfactorily reproducible independently of the differing hair structures to which they are applied.
- the azo dye compound of formula I are produced in good yield by simple chemical reactions, for example according to the methods described in German Patent DE-PS 543 288 or German Published Patent Application DE-OS 4 219 738, and have an exceptional stability to reducing agents.
- 20 g of the above hair dye gel composition are mixed with 20 g of a 9% by weight hydrogen peroxide solution. Subsequently the mixture so obtained is applied to gray human hair and allowed to act on the hair for an acting time of thirty minutes at 40° C. The hair is then rinsed with water and dried.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
A--N=N--B (I),
______________________________________
Example 1
Hair Dye Gel Composition
______________________________________
1.0 g 4-aminophenol
0.4 g α-naphthol
0.4 g 3-amino-6-methyl-phenol
0.3 g 2,6-diamino-3-[3'-azopyridyl]pyridine
0.1 g resorcinol
0.1 g 2,5-diaminotoluene sulfate
15.0 g oleic acid
8.0 g isopropanol
6.0 g ammonia (25 percent by weight aqueous solution)
3.0 g glycerol
0.3 g ascorbic acid
0.1 g sodium bisulfite
65.3 g water
100.0
______________________________________
______________________________________
Example 2 Hair Dye Cream Composition
______________________________________
0.32 g 2,5-diaminotoluene sulfate
0.30 g 4-amino-4'-[N,N-bis-
(2"-hydroxyethyl)amino]azobenzene
0.20 g 2-amino-6-chloro-4-nitrophenol
0.18 g 2,6-dihydroxytoluene
15.00 g a mixture of cetyl stearyl alcohol and
sodium lauryl sulfate (90:10)
(Lanette.sup.R of Henkel kGaA/Germany)
3.50 g sodium diglycol lauryl ether sulfate
(20-percent aqueous solution)
2.40 g sodium hydroxide (20% aqueous solution)
0.40 g sodium bisulfite
0.20 g ascorbic acid
0.20 g monoethanolamine
77.30 g water
100.0
______________________________________
Claims (23)
A--N=N--B (I),
A--N=N--B (I),
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19515903.9 | 1995-04-29 | ||
| DE19515903A DE19515903C2 (en) | 1995-04-29 | 1995-04-29 | Means and methods for oxidative coloring of hair |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5637115A true US5637115A (en) | 1997-06-10 |
Family
ID=7760764
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/586,300 Expired - Lifetime US5637115A (en) | 1995-04-29 | 1996-01-16 | Oxidation hair dye compositions containing developers, couplers, and AZO dyes |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5637115A (en) |
| EP (1) | EP0739622B1 (en) |
| BR (1) | BR9602056A (en) |
| DE (2) | DE19515903C2 (en) |
| ES (1) | ES2097715T3 (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5785961A (en) * | 1995-03-28 | 1998-07-28 | Shiseido Company, Ltd. | Mixing-at the time of use-type hair-treating composition |
| US5879412A (en) * | 1996-12-23 | 1999-03-09 | L'oreal | Compositions and processes for dyeing keratin fibers with an oxidation base, a coupler, a cationic direct dye, and an oxidizing agent |
| US5919273A (en) * | 1996-12-23 | 1999-07-06 | L'oreal | Compositions and processes for dyeing keratin fibers with an oxidation base, a coupler, a cationic direct dye, and an oxidizing agent |
| FR2773471A1 (en) * | 1998-01-13 | 1999-07-16 | Oreal | Composition for dyeing keratinic fibers, especially human hair |
| US5993490A (en) * | 1996-12-23 | 1999-11-30 | L'oreal | Composition for the oxidation dyeing of keratin fibers containing a cationic direct dye and dyeing process using this composition |
| US6001135A (en) * | 1996-12-23 | 1999-12-14 | L'oreal | Compositions and processes for dyeing keratin fibers with cationic direct dyes, oxidation bases, and oxidizing agents |
| US6440177B1 (en) | 2000-01-19 | 2002-08-27 | Artec Systems Group | One-step bleach and coloring composition for hair and method of using same |
| RU2197948C2 (en) * | 1999-01-19 | 2003-02-10 | Л`Ореаль | Application of cationic phenylazobenzene compounds for staining keratin fibers, staining composites and methods of staining |
| US6554871B2 (en) * | 1996-10-18 | 2003-04-29 | Wella Ag | Oxidative hair dye precursor compositions containing 4-5-diaminopyrazole, 5-amino-2-methylphenol and m-phenylenediamine compounds and method of dyeing hair |
| US20040019982A1 (en) * | 2002-05-28 | 2004-02-05 | Kao Corporation | Hair dye composition |
| US20050193504A1 (en) * | 2004-03-04 | 2005-09-08 | Glenn Robert W.Jr. | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| US20090185699A1 (en) * | 2006-05-17 | 2009-07-23 | Sung-Ho Kim | Bone conduction headset |
| US20090320215A1 (en) * | 2006-08-10 | 2009-12-31 | Jack Massoni | Catalyzed air oxidation haircolor |
| US9889080B2 (en) | 2015-05-07 | 2018-02-13 | Celeb LLC | Color depositing shampoo |
| US10245221B2 (en) | 2015-05-07 | 2019-04-02 | Celeb LLC | Stabilized color depositing shampoo |
| US20220040075A1 (en) * | 2018-12-21 | 2022-02-10 | L'oreal | Process for dyeing keratin materials using a direct dye and an unsaturated heterocyclic salt, and composition comprising same |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2776185B1 (en) * | 1998-03-20 | 2001-01-26 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
| FR2776186B1 (en) * | 1998-03-20 | 2001-01-26 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
| JP2001316232A (en) * | 2000-05-11 | 2001-11-13 | Kao Corp | Hair dye |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3368941A (en) * | 1963-09-04 | 1968-02-13 | Therachemie Chem Therapeut | Azo compounds for dyeing human hair |
| US4025301A (en) * | 1974-09-27 | 1977-05-24 | Societe Anonyme Dite: L'oreal | Azo dyes derived from 3-amino pyridine in hair dye compositions |
| US4289495A (en) * | 1977-08-19 | 1981-09-15 | L'oreal | Oxidative dye compositions containing a 2,5-dihydroxyphenylalkanoic acid or salts thereof as antioxidant |
| US4886517A (en) * | 1984-10-01 | 1989-12-12 | L'oreal | Dyeing composition for human hair containing an azo dye |
| DE3942315A1 (en) * | 1989-12-21 | 1991-06-27 | Wella Ag | FOAM SHAPED HAIR TONENT |
| US5226924A (en) * | 1990-10-12 | 1993-07-13 | L'oreal | 1,4-di(mono- or poly) hydroxyalkylamino-9,10-anthraquinones for dyeing human keratinous fibres, cosmetic composition containing them in combination with azo and nitrobenzene dyes, and hair-dyeing process using them |
| DE4219738A1 (en) * | 1992-06-17 | 1993-12-23 | Wella Ag | Hair Dye |
| EP0601302A1 (en) * | 1992-12-07 | 1994-06-15 | Wella Aktiengesellschaft | Hair dyeing composition containing 3-pyridinazo dyes and novel 3-pyridazo dyes |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE543288C (en) | 1928-12-12 | 1932-02-04 | Schering Kahlbaum Ag | Process for the preparation of new heterocyclic compounds |
| FR1585308A (en) * | 1967-10-10 | 1970-01-16 | ||
| DE3914253A1 (en) * | 1989-04-29 | 1990-10-31 | Wella Ag | OXIDATING HAIR AGENTS BASED ON 4-AMINOPHENOL DERIVATIVES AND NEW 4-AMINOPHENOL DERIVATIVES |
-
1995
- 1995-04-29 DE DE19515903A patent/DE19515903C2/en not_active Expired - Fee Related
- 1995-12-02 EP EP95119004A patent/EP0739622B1/en not_active Expired - Lifetime
- 1995-12-02 ES ES95119004T patent/ES2097715T3/en not_active Expired - Lifetime
- 1995-12-02 DE DE59509353T patent/DE59509353D1/en not_active Expired - Lifetime
-
1996
- 1996-01-16 US US08/586,300 patent/US5637115A/en not_active Expired - Lifetime
- 1996-04-25 BR BR9602056A patent/BR9602056A/en not_active Application Discontinuation
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3368941A (en) * | 1963-09-04 | 1968-02-13 | Therachemie Chem Therapeut | Azo compounds for dyeing human hair |
| US4025301A (en) * | 1974-09-27 | 1977-05-24 | Societe Anonyme Dite: L'oreal | Azo dyes derived from 3-amino pyridine in hair dye compositions |
| US4289495A (en) * | 1977-08-19 | 1981-09-15 | L'oreal | Oxidative dye compositions containing a 2,5-dihydroxyphenylalkanoic acid or salts thereof as antioxidant |
| US4886517A (en) * | 1984-10-01 | 1989-12-12 | L'oreal | Dyeing composition for human hair containing an azo dye |
| DE3942315A1 (en) * | 1989-12-21 | 1991-06-27 | Wella Ag | FOAM SHAPED HAIR TONENT |
| US5226924A (en) * | 1990-10-12 | 1993-07-13 | L'oreal | 1,4-di(mono- or poly) hydroxyalkylamino-9,10-anthraquinones for dyeing human keratinous fibres, cosmetic composition containing them in combination with azo and nitrobenzene dyes, and hair-dyeing process using them |
| DE4219738A1 (en) * | 1992-06-17 | 1993-12-23 | Wella Ag | Hair Dye |
| US5409502A (en) * | 1992-06-17 | 1995-04-25 | Wella Aktiengesellschaft | Hair dye composition containing a 4'-amino-2-halogen-4-{bis-(-hydroxyethyl)amino} azobenzene compound |
| EP0601302A1 (en) * | 1992-12-07 | 1994-06-15 | Wella Aktiengesellschaft | Hair dyeing composition containing 3-pyridinazo dyes and novel 3-pyridazo dyes |
Non-Patent Citations (2)
| Title |
|---|
| Hair Dyes, J.C. Johnson, 1973, pp. 1 139. * |
| Hair Dyes, J.C. Johnson, 1973, pp. 1-139. |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5785961A (en) * | 1995-03-28 | 1998-07-28 | Shiseido Company, Ltd. | Mixing-at the time of use-type hair-treating composition |
| US6554871B2 (en) * | 1996-10-18 | 2003-04-29 | Wella Ag | Oxidative hair dye precursor compositions containing 4-5-diaminopyrazole, 5-amino-2-methylphenol and m-phenylenediamine compounds and method of dyeing hair |
| US6001135A (en) * | 1996-12-23 | 1999-12-14 | L'oreal | Compositions and processes for dyeing keratin fibers with cationic direct dyes, oxidation bases, and oxidizing agents |
| US5879412A (en) * | 1996-12-23 | 1999-03-09 | L'oreal | Compositions and processes for dyeing keratin fibers with an oxidation base, a coupler, a cationic direct dye, and an oxidizing agent |
| US5919273A (en) * | 1996-12-23 | 1999-07-06 | L'oreal | Compositions and processes for dyeing keratin fibers with an oxidation base, a coupler, a cationic direct dye, and an oxidizing agent |
| US5993490A (en) * | 1996-12-23 | 1999-11-30 | L'oreal | Composition for the oxidation dyeing of keratin fibers containing a cationic direct dye and dyeing process using this composition |
| US20050193503A1 (en) * | 1998-01-13 | 2005-09-08 | L'oreal S.A. | Composition for the oxidation dyeing of keratinous fibres containing a laccase and dyeing method using this composition |
| WO1999036034A1 (en) * | 1998-01-13 | 1999-07-22 | L'oreal | Keratinous fibre dyeing composition containing a laccase and dyeing method using same |
| FR2773471A1 (en) * | 1998-01-13 | 1999-07-16 | Oreal | Composition for dyeing keratinic fibers, especially human hair |
| RU2197948C2 (en) * | 1999-01-19 | 2003-02-10 | Л`Ореаль | Application of cationic phenylazobenzene compounds for staining keratin fibers, staining composites and methods of staining |
| US6440177B1 (en) | 2000-01-19 | 2002-08-27 | Artec Systems Group | One-step bleach and coloring composition for hair and method of using same |
| US7083655B2 (en) * | 2002-05-28 | 2006-08-01 | Kao Corporation | Hair dye composition |
| US20040019982A1 (en) * | 2002-05-28 | 2004-02-05 | Kao Corporation | Hair dye composition |
| AU2005221648B2 (en) * | 2004-03-04 | 2008-05-29 | The Procter And Gamble Company | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| US7351266B2 (en) | 2004-03-04 | 2008-04-01 | The Procter & Gamble Company | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| US20050193504A1 (en) * | 2004-03-04 | 2005-09-08 | Glenn Robert W.Jr. | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| US20080134450A1 (en) * | 2004-03-04 | 2008-06-12 | Robert Wayne Glenn | Keratin Dyeing Compounds, Keratin Dyeing Compositions Containing Them, And Use Thereof |
| US7468080B2 (en) | 2004-03-04 | 2008-12-23 | The Procter & Gamble Company | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof |
| US20090185699A1 (en) * | 2006-05-17 | 2009-07-23 | Sung-Ho Kim | Bone conduction headset |
| US20090320215A1 (en) * | 2006-08-10 | 2009-12-31 | Jack Massoni | Catalyzed air oxidation haircolor |
| US7758659B2 (en) | 2006-08-10 | 2010-07-20 | Combe Incorporated | Catalyzed air oxidation haircolor |
| US9889080B2 (en) | 2015-05-07 | 2018-02-13 | Celeb LLC | Color depositing shampoo |
| US10245221B2 (en) | 2015-05-07 | 2019-04-02 | Celeb LLC | Stabilized color depositing shampoo |
| US20220040075A1 (en) * | 2018-12-21 | 2022-02-10 | L'oreal | Process for dyeing keratin materials using a direct dye and an unsaturated heterocyclic salt, and composition comprising same |
Also Published As
| Publication number | Publication date |
|---|---|
| DE19515903A1 (en) | 1996-10-31 |
| EP0739622B1 (en) | 2001-06-20 |
| ES2097715T1 (en) | 1997-04-16 |
| ES2097715T3 (en) | 2001-10-16 |
| EP0739622A1 (en) | 1996-10-30 |
| DE19515903C2 (en) | 1998-04-16 |
| BR9602056A (en) | 1998-04-07 |
| DE59509353D1 (en) | 2001-07-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5637115A (en) | Oxidation hair dye compositions containing developers, couplers, and AZO dyes | |
| US5766576A (en) | Oxidation hair dye compositions containing 3,4,5-triaminopyrazole derivatives and 3,4,5-triaminopyrazole derivatives | |
| RU2027429C1 (en) | Agent for oxidative hairs staining | |
| US4883656A (en) | Composition and method for the oxidative dyeing of hair | |
| US6074438A (en) | Hair dyeing compositions containing 2-chloro- and 2,6-dichloro-4-aminophenol and phenylpyrazolones | |
| US6554871B2 (en) | Oxidative hair dye precursor compositions containing 4-5-diaminopyrazole, 5-amino-2-methylphenol and m-phenylenediamine compounds and method of dyeing hair | |
| US6740127B2 (en) | Agent and method for coloring keratin fibres | |
| JP2000502367A (en) | Agents and methods for dyeing keratin fibers | |
| GB2104922A (en) | Medium and process for the dyeing of hair | |
| JPH07304640A (en) | Oxidative dyeing composition of keratin fiber and dyeing method using the dyeing composition | |
| WO1986002829A1 (en) | Oxidation-type hair-dyeing means based on 4-amino-2-hydroxyalkyl-phenols | |
| US5409503A (en) | Oxidation hair dye with a content of 5-aminophenyl derivatives, process for oxidative dyeing of hair and new 5-aminophenol derivatives | |
| US4543425A (en) | 1,3-Diamino-4-(2',2',2',-trifluoroethoxy)-benzene, method of producing the same, and hair coloring composition containing the same | |
| JPH04117322A (en) | Oxidative hair dye and hair dyeing method | |
| US5224965A (en) | Composition for the oxidative dyeing of hair and new 5-halogen-2,4-diamino alkylbenzenes | |
| US6099591A (en) | Method and composition for hair coloring using green tea polyphenols | |
| JPH05186319A (en) | Oxidative hair dye | |
| US4325704A (en) | Hair dyes | |
| US5645610A (en) | Substituted 2-alkylamino-4-amino-1-alkylbenzene compounds and oxidation hair dye compositions based on said compounds | |
| DE68903471T2 (en) | TRIALCOXY-SUBSTITUTED M-PHENYLENE DIAMINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A COUPLER IN THE OXYDATION DYEING OF KERATINIC FIBERS, PARTICULARLY HUMAN HAIR. | |
| WO2005023209A1 (en) | Agent and method for dyeing keratin fibers | |
| US4452603A (en) | Process for dyeing hair and composition therefor | |
| US4828568A (en) | Oxidation hair-dyeing preparations | |
| DE4123941A1 (en) | METHOD FOR THE OXIDATIVE COLORING OF HAIR | |
| US5542953A (en) | 5-halogen-2,4-Bis (alkylamino)-1-alkylbenzenes and hair dye compositions containing same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: WELLA AKTIENGESELLSCHAFT, GERMANY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BALZER, WOLFGANG R.;BRAUN, HANS-JUERGEN;REEL/FRAME:007840/0714 Effective date: 19960110 |
|
| FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
| FPAY | Fee payment |
Year of fee payment: 4 |
|
| FPAY | Fee payment |
Year of fee payment: 8 |
|
| FPAY | Fee payment |
Year of fee payment: 12 |
|
| AS | Assignment |
Owner name: WELLA GMBH, GERMANY Free format text: CHANGE OF NAME;ASSIGNOR:WELLA AG;REEL/FRAME:027240/0338 Effective date: 20110223 |
|
| AS | Assignment |
Owner name: HFC PRESTIGE INTERNATIONAL HOLDING SWITZERLAND S.A Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WELLA GMBH;REEL/FRAME:040420/0478 Effective date: 20160921 |